Peroxisomal Bifunctional Enzyme anticorps (Middle Region)

N° du produit ABIN5514454

L’anticorps anti-Peroxisomal Bifunctional Enzyme Polyclonal produit chez le Lapin a été validé pour WB. Il convient pour la détection de Peroxisomal Bifunctional Enzyme dans des échantillons provenant de Humain. }

Aperçu rapide pour Peroxisomal Bifunctional Enzyme anticorps (Middle Region) (ABIN5514454)

Antigène: Peroxisomal Bifunctional Enzyme (ECHP)

Reactivité: Humain

Hôte: Lapin

Clonalité: Polyclonal

Application: Western Blotting (WB)

Détail du produit anti-Peroxisomal Bifunctional Enzyme anticorps

Épitope: Middle Region

Séquence: VIAVDSDKNQ LATANKMITS VLEKEASKMQ QSGHPWSGPK PRLTSSVKEL

Attributs du produit: This is a rabbit polyclonal antibody against ECHP. It was validated on Western Blot.

Purification: Affinity purified

Immunogène: The immunogen is a synthetic peptide directed towards the middle region of Human ECHP

Information d'application

Indications d'application: Optimal working dilution should be determined by the investigator.

Restrictions: For Research Use only

Stockage

Format: Liquid

Buffer: Liquid. Purified antibody supplied in 1x PBS buffer with 0.09 % (w/v) sodium azide and 2 % sucrose.

Agent conservateur: Sodium azide

Précaution d'utilisation: This product contains Sodium azide: a POISONOUS AND HAZARDOUS SUBSTANCE which should be handled by trained staff only.

Stock: -20 °C

Stockage commentaire: For short term use, store at 2-8°C up to 1 week. For long term storage, store at -20°C in small aliquots to prevent freeze-thaw cycles.

Détails sur Peroxisomal Bifunctional Enzyme

Antigène: Peroxisomal Bifunctional Enzyme (ECHP)

Autre désignation: ECHP

Sujet: The protein encoded by this gene is a bifunctional enzyme and is one of the four enzymes of the peroxisomal beta-oxidation pathway. The N-terminal region of the encoded protein contains enoyl-CoA hydratase activity while the C-terminal region contains 3-hydroxyacyl-CoA dehydrogenase activity. Defects in this gene are a cause of peroxisomal disorders such as Zellweger syndrome. Two transcript variants encoding different isoforms have been found for this gene.

Alias Symbols: EHHADH, ECHD,

Protein Size: 723

ID gène: 1962

NCBI Accession: NP_001957

UniProt: Q08426